Allele Registry

Canonical Allele Identifier: PA2499247999

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001325045

RCV002466661

ClinVar Variation:

1024818

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Pro94Ser	CA378921072 NM_001318054.2:c.280C>T